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Chloro-2-thiophenyl-3-propionitrile is a chemical compound with the molecular formula C6H4ClNS. It is a derivative of 2-thiophenepropionitrile, featuring a chlorine atom attached to the thiophene ring and a nitrile group (CN) at the 3-position. chloro-2 thiophenyl-3 propionitrile is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, it is often used in the development of new compounds with specific properties. However, it is essential to handle chloro-2-thiophenyl-3-propionitrile with care, as it may have toxic or hazardous effects on human health and the environment.

1424-49-3

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1424-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1424-49-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1424-49:
(6*1)+(5*4)+(4*2)+(3*4)+(2*4)+(1*9)=63
63 % 10 = 3
So 1424-49-3 is a valid CAS Registry Number.

1424-49-3Relevant academic research and scientific papers

A new synthesis of 1-phenylthio- and 1-alkylamino-4-nitrobuta-1,3-dienes

Ono, Noboru,Matsumoto, Koji,Ogawa, Takuji,Tani, Hiroyuki,Uno, Hidemitsu

, p. 1905 - 1910 (2007/10/03)

A new synthesis of push-pull dienes such as 4-nitro-1-phenylthiopenta-1,3-diene 4 and 1-dialkylamino-4-nitropenta-1,3-diene 5, is described. The X-ray crystal analysis shows that 4-nitro-1-(pynolidin-1-yl)penta-1,3-diene 5a is essentially planar in an E,E

Dienophilie des olefines captodatives: influence de l'encombrement sterique des α-alkylthioacrylonitriles sur la stereoselectivite des reactions de Diels-Alder

Boucher, Jean-Luc,Stella, Lucien

, p. 276 - 282 (2007/10/02)

The Diels-Alder reaction of cyclopentadiene with a series of α-alkyl-(or aryl)-thioacrylonitriles were investigated.The spontaneous cycloaddition occurs at room temperature affording adducts in excellent yield.The stereochemical assignments of the adducts

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